Site‐Specific Phosphorylation of Huntingtin Exon 1 Recombinant Proteins Enabled by the Discovery of Novel Kinases - Chiki - 2021 - ChemBioChem - Wiley Online Library
Heterogeneous Nuclear Ribonucleoproteins: Implications in Neurological Diseases | SpringerLink
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Suppression of toxicity of the mutant huntingtin protein by its interacting compound, desonide | PNAS
Dynamics of the Proline-Rich C-Terminus of Huntingtin Exon-1 Fibrils. - Abstract - Europe PMC
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RNA toxicity and foci formation in microsatellite expansion diseases. - Abstract - Europe PMC
Targeting strategy for SP-D gene disruption and confirmation of the... | Download Scientific Diagram
Genes | Free Full-Text | Antisense Transcription across Nucleotide Repeat Expansions in Neurodegenerative and Neuromuscular Diseases: Progress and Mysteries
RNA and Disease: Cell
TNFR1-d2 carrying the p.(Thr79Met) pathogenic variant is a potential novel actor of TNFα/TNFR1 signalling regulation in the pathophysiology of TRAPS | Scientific Reports
Absence of perilipin results in leanness and reverses obesity in Leprdb/db mice | Nature Genetics
TNFR1-d2 carrying the p.(Thr79Met) pathogenic variant is a potential novel actor of TNFα/TNFR1 signalling regulation in the pathophysiology of TRAPS | Scientific Reports
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Application of CRISPR-Cas9-Mediated Genome Editing for the Treatment of Myotonic Dystrophy Type 1: Molecular Therapy
Genes containing hexanucleotide repeats resembling C9ORF72 and expressed in the central nervous system are frequent in the human genome - ScienceDirect
Sam68 sequestration and partial loss of function are associated with splicing alterations in FXTAS patients | The EMBO Journal
Insects | Free Full-Text | CRISPR/Cas9-Mediated Mutagenesis of Abdominal-A and Ultrabithorax in the Asian Corn Borer, Ostrinia furnacalis
